Evidence map›Paper›PMID 37935783›Full record

ArticleBone marrow transplantation2024

AKI treated with kidney replacement therapy in critically Ill allogeneic hematopoietic stem cell transplant recipients.

Helena Kim, Rafia Ali, Samuel Short, Sarah Kaunfer, Shobana Krishnamurthy, Lavanya Durai, Osman Yilmam, Tushar Shenoy, Audrey E Monson, Charlotte Thomas and 10 more

Abstract read
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.0field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 4 institutions in 1 country.

Helena Kim *Division of Renal Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Rafia Ali *Division of Renal Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Samuel ShortLarner College of Medicine, University of Vermont, Burlington, VT, USA.
Sarah KaunferDivision of Renal Medicine, Brigham and Women's Hospital, Boston, MA, USA.ORCID 0000-0003-3335-1408
Shobana KrishnamurthyDivision of Renal Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Lavanya DuraiDivision of Renal Medicine, Brigham and Women's Hospital, Boston, MA, USA.ORCID 0009-0005-6547-2564
Osman YilmamDivision of Renal Medicine, Brigham and Women's Hospital, Boston, MA, USA.ORCID 0000-0001-8202-1320
Tushar ShenoyDivision of Renal Medicine, Brigham and Women's Hospital, Boston, MA, USA.ORCID 0000-0002-5660-6111
Audrey E MonsonDivision of Renal Medicine, Brigham and Women's Hospital, Boston, MA, USA.ORCID 0009-0003-9287-9680
Charlotte ThomasDivision of Renal Medicine, Brigham and Women's Hospital, Boston, MA, USA.ORCID 0000-0002-5602-0890
Isabel ParkDivision of Renal Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Dylan MartiniDepartment of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Richard NewcombDivision of Hematology & Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Roman M ShapiroDivision of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Robert J SoifferDivision of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0002-5810-1192
Zachariah DeFilippHematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA, USA.ORCID 0000-0002-7994-8974
Rebecca M BaronDivision of Pulmonary and Critical Care Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Shruti GuptaDivision of Renal Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Meghan E SiseDivision of Nephrology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.ORCID 0000-0002-4327-9713
David E LeafDivision of Renal Medicine, Brigham and Women's Hospital, Boston, MA, USA. DELEAF@bwh.harvard.edu.ORCID 0000-0001-7875-090X
Brigham and Women's Hospital · USMassachusetts General Hospital · USDana-Farber Cancer Institute · USUniversity of Vermont · US

Funding

Mechanisms driving acute and chronic kidney function decline after immune checkpoint inhibitor therapy for cancerR01DK130839 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Meghan E. Sise · 2022 to 2026
$3.6M
Deferoxamine for the Prevention of Acute Kidney InjuryR01DK125786 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI LEAF, DAVID EVAN · 2020 to 2024
$3.5M
Hepcidin-Ferroportin-Iron Axis in Cardiac Surgery-associated Acute Kidney InjuryR01DK126685 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI LEAF, DAVID EVAN · 2022 to 2025
$3.3M
Therapeutic modulation of zinc for lung injury and mechanobiologyR01HL142093 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI BARON, REBECCA M, TSCHUMPERLIN, DANIEL J. · 2019 to 2022
$2.8M
Precision Medicine Approach to Vitamin D3 Administration in Critical IllnessR01HL144566 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI LEAF, DAVID EVAN · 2019 to 2022
$1.8M
Novel Pathways and Therapeutic Targets for Cisplatin-Associated Acute Kidney InjuryK23DK125672 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI Shruti Gupta · 2022 to 2026
$998k
NHLBI NIH HHS R01 HL142093NHLBI NIH HHS R01 HL144566NIDDK NIH HHS K23 DK125672NIDDK NIH HHS R01 DK125786NIDDK NIH HHS R01 DK126685NIDDK NIH HHS R01 DK130839
6 · The paper itself

Abstract

Acute kidney injury (AKI) is a frequent complication following allogeneic hematopoietic stem cell transplantation (allo-HSCT), but few studies have focused on AKI treated with kidney replacement therapy (AKI-KRT), particularly among critically ill patients. We investigated the incidence, risk factors, and 90-day mortality associated with AKI-KRT in 529 critically ill adult allo-HSCT recipients admitted to the ICU within 1-year post-transplant at two academic medical centers between 2011 and 2021. AKI-KRT occurred in 111 of the 529 patients (21.0%). Lower baseline eGFR, veno-occlusive disease, thrombotic microangiopathy, admission to an ICU within 90 days post-transplant, and receipt of invasive mechanical ventilation (IMV), total bilirubin ≥5.0 mg/dl, and arterial pH <7.40 on ICU admission were each associated with a higher risk of AKI-KRT. Of the 111 patients with AKI-KRT, 97 (87.4%) died within 90 days. Ninety-day mortality was 100% in each of the following subgroups: serum albumin ≤2.0 g/dl, total bilirubin ≥7.0 mg/dl, arterial pH ≤7.20, IMV with moderate-to-severe hypoxemia, and ≥3 vasopressors/inotropes at KRT initiation. AKI-KRT was associated with a 6.59-fold higher adjusted 90-day mortality in critically ill allo-HSCT vs. non-transplanted patients. Short-term mortality remains exceptionally high among critically ill allo-HSCT patients with AKI-KRT, highlighting the importance of multidisciplinary discussions prior to KRT initiation.

Indexed as

Acute Kidney InjuryHematopoietic Stem Cell TransplantationAdultBilirubinCritical IllnessHumansRenal Replacement TherapyRetrospective StudiesBilirubin

Identifiers

PMID37935783
OpenAlexW4388452636

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.